추천 제품
형태
powder
제조업체/상표
Avanti Research™ - A Croda Brand
포장
1 ea of 1 × (with stopper and crimp cap (LM1900-1EA))
응용 분야
lipidomics
metabolomics
배송 상태
dry ice
저장 온도
−20°C
SMILES string
[H][C@@](COP([O-])(O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](OP([O-])(O)=O)[C@H]1O)=O)(OC(CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC)=O)COC(CCCCCCCCCCCCCCCC)=O.[NH4+].[NH4+]
일반 설명
17:0-20:4 PI(3)P, phosphatidylinositol 3?phosphate, is the predominant phosphoinositide localized in endosomes and yeast vacuoles. It is synthesized by phosphatidylinositol 3?kinase (PI3K) from phosphatidylinositol.
애플리케이션
17:0-20:4 PI(3)P has been used as an internal standard for targeted lipidomic analysis.
생화학적/생리학적 작용
17:0-20:4 PI(3)P plays a vital role in intracellular membrane trafficking and recruitment of effector proteins, which possess PI(3)P-binding motifs to membranes. It also regulates the formation of autophagosomes.
포장
2 mL Amber Serum Vial with Stopper and Crimp Cap (LM1900-1EA)
법적 정보
Avanti Research is a trademark of Avanti Polar Lipids, LLC
Storage Class Code
11 - Combustible Solids
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
The spastic paraplegia-associated phospholipase DDHD1 is a primary brain phosphatidylinositol lipase
Molecules (Basel), 57(39), 5759-5767 (2018)
The Role of PI3P Phosphatases in the Regulation of Autophagy
Febs Letters, 584(7), 1313-1318 (2010)
The phosphatidylinositol 3?phosphate?binding FYVE finger
Febs Letters, 513(1), 77-84 (2002)
Proceedings of the National Academy of Sciences of the United States of America, 97(16), 8910-8915 (2000-07-20)
The lipid second messenger phosphatidylinositol 3-phosphate [PI(3)P] plays a crucial role in intracellular membrane trafficking. We report here that myotubularin, a protein tyrosine phosphatase required for muscle cell differentiation, is a potent PI(3)P phosphatase. Recombinant human myotubularin specifically dephosphorylates PI(3)P
Biochemistry, 57(39), 5759-5767 (2018-09-18)
Deleterious mutations in the serine hydrolase DDHD domain containing 1 (DDHD1) cause the SPG28 subtype of the neurological disease hereditary spastic paraplegia (HSP), which is characterized by axonal neuropathy and gait impairments. DDHD1 has been shown to display PLA1-type phospholipase
자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..
고객지원팀으로 연락바랍니다.